Homology of Ti α-subunit of a T-cell antigen-MHC receptor with immunoglobulin

M. Fabbi, O. Acuto, J. E. Smart, E. L. Reinherz

Research output: Contribution to journalArticlepeer-review

Abstract

Human T-cell receptors for antigen and major histocompatibility complex (MHC) determinants have now been defined on inducer, suppressor, and class 1 and class 2 MHC-specific cytotoxic T lymphocytes as T3-associated clonotypic molecules (Ti) of relative molecular mass 90,000 (90K) composed of one 49-54K α- and one 43K β-subunit which are disulphide-linked. In the case of the Ti β-subunit, N-terminal amino acid sequencing and molecular cloning techniques led recently to identification of the Ti β-gene and showed that T-specific V, D, J and C segments fuse to form an active β-gene. So far, however, there have been little structural data available on the Ti α-subunit. Here we have derived the amino acid sequence of a portion of the Ti α-subunit by CNBr fragmentation. Sequence analysis reveals ~40% homology between the Ti α-subunit fragment and the third framework of the variable region of immunoglobulin light and heavy chains, supporting the notion that the Ti α-subunit is a member of the immunoglobulin-Ti β-gene family.

Original languageEnglish
Pages (from-to)269-271
Number of pages3
JournalNature
Volume312
Issue number5991
Publication statusPublished - 1984

ASJC Scopus subject areas

  • General

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